Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Pierre A. Russo"'
Publikováno v:
Annals of Hepatology, Vol 16, Iss 3, Pp 465-468 (2017)
Progressive Familial Intrahepatic Cholestasis type 2 (PFIC2) is a rare cholestatic disorder diagnosed in infancy or childhood that can lead to severe hepatic fibrosis and liver failure. Mutations in the ABCB11 gene result in a deficiency of the bile
Externí odkaz:
https://doaj.org/article/ce673812c5bb45b1833dfffc1742a75a
Autor:
Iris E.M. de Jong, Mallory L. Hunt, Dongning Chen, Yu Du, Jessica Llewellyn, Kapish Gupta, Dorothea Erxleben, Felipe Rivas, Adam R. Hall, Emma E. Furth, Ali Naji, Chengyang Liu, Abhishek Dhand, Jason Burdick, Marcus G. Davey, Alan W. Flake, Robert J. Porte, Pierre A. Russo, J. William Gaynor, Rebecca G. Wells
IntroductionBiliary atresia (BA) is an obstructive cholangiopathy that initially affects the extrahepatic bile ducts (EHBDs) of neonates. The etiology is uncertain, but evidence points to a prenatal cause; however, the response of the fetal EHBD to i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::272df5e6ba1a178955de99f3f74a99e8
https://doi.org/10.1101/2022.12.15.520656
https://doi.org/10.1101/2022.12.15.520656
Publikováno v:
The American journal of surgical pathology. 46(10)
Pseudoacini are generally a morphologic feature of hepatocellular carcinoma (HCC), being absent or rare in benign hepatocytic tumors, such as hepatocellular adenoma. However, rarely these can be seen in focal nodular hyperplasia (FNH) and may pose di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::349dc205abf97f7205edbfddb046ef5f
https://pubmed.ncbi.nlm.nih.gov/35749760
https://pubmed.ncbi.nlm.nih.gov/35749760
Autor:
Jan Marc Orenstein, Stanford T Shulman, Linda M Fox, Susan C Baker, Masato Takahashi, Tricia R Bhatti, Pierre A Russo, Gary W Mierau, Jean Pierre de Chadarévian, Elizabeth J Perlman, Cynthia Trevenen, Alexandre T Rotta, Mitra B Kalelkar, Anne H Rowley
Publikováno v:
PLoS ONE, Vol 7, Iss 6, p e38998 (2012)
Kawasaki disease is recognized as the most common cause of acquired heart disease in children in the developed world. Clinical, epidemiologic, and pathologic evidence supports an infectious agent, likely entering through the lung. Pathologic studies
Externí odkaz:
https://doaj.org/article/c694df9895ed4f4ca97e4c4af4795368
Autor:
Anne H Rowley, Susan C Baker, Stanford T Shulman, Francesca L Garcia, Linda M Fox, Ian M Kos, Susan E Crawford, Pierre A Russo, Rashid Hammadeh, Kei Takahashi, Jan M Orenstein
Publikováno v:
PLoS ONE, Vol 3, Iss 2, p e1582 (2008)
Kawasaki Disease (KD) is the most common cause of acquired heart disease in children in developed nations. The KD etiologic agent is unknown but likely to be a ubiquitous microbe that usually causes asymptomatic childhood infection, resulting in KD o
Externí odkaz:
https://doaj.org/article/6a6cc1270efd4073b27e9e43e2a7a2cb
Autor:
Patrícia, Costa-Reis, Pierre A, Russo, Zhe, Zhang, Lucrezia, Colonna, Kelly, Maurer, Stefania, Gallucci, Steffan W, Schulz, Adnan N, Kiani, Michelle, Petri, Kathleen E, Sullivan
Publikováno v:
Arthritis Rheumatol
OBJECTIVE. To understand the roles of microRNAs (miRNAs) in proliferative lupus nephritis (LN). METHODS. A high-throughput analysis of the miRNA pattern of the kidneys of LN patients and controls was performed by molecular digital detection. Urinary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e8d34fc8f1d78e989d672ebcf0bbf96a
https://pubmed.ncbi.nlm.nih.gov/26016809
https://pubmed.ncbi.nlm.nih.gov/26016809
Publikováno v:
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society. 2(1)
Autoimmune enteropathy (AIE) is an entity reported primarily in infancy, resulting in intractable diarrhea and associated with small bowel villous atrophy and the presence of circulating anti-enterocyte (AEA) antibodies. It is a multisystem disorder
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c97827e43e3d1e898dac7e86de53ae6
https://pubmed.ncbi.nlm.nih.gov/9841709
https://pubmed.ncbi.nlm.nih.gov/9841709
Autor:
Feoli-Fonseca, Juan Carlos, Filion, Mario, Brochu, Pierre, Simard, Pierre, Luc, L. Oligny, Pierre, A. Russo, Wagner, V. Yotov
Publikováno v:
Diagnostic Molecular Pathology; Dec1998, Vol. 7 Issue 6, p317-323, 7p
Autor:
Feoli-Fonseca, Juan Carlos, Filion, Mario, Brochu, Pierre, Simard, Pierre, Luc, L. Oligny, Pierre, A. Russo, Wagner, V. Yotov
Publikováno v:
Diagnostic Molecular Pathology; December 1998, Vol. 7 Issue: 6 p317-323, 7p